Ophthalmological ciliopathies

Gene: CRX

Red List (low evidence)

CRX (cone-rod homeobox)
EnsemblGeneIds (GRCh38): ENSG00000105392
EnsemblGeneIds (GRCh37): ENSG00000105392
OMIM: 602225, Gene2Phenotype
CRX is in 12 panels

1 review

Alice Gardham (Genomics England)

Comment when marking as ready: Leber's congenital amaurosis not included on this panel
Created: 23 Jan 2017, 4:28 p.m.

History Filter Activity

8 Jul 2019, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set Phenotypes

Ivone Leong (Genomics England Curator)

gene: CRX was added gene: CRX was added to Ophthalmological ciliopathies. Sources: Emory Genetics Laboratory,Expert Review Red Mode of inheritance for gene: CRX was set to Phenotypes for gene: CRX were set to Ciliopathies